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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2004 1
2005 2
2006 2
2007 1
2009 3
2010 2
2011 2
2012 2
2013 3
2014 3
2015 3
2016 1
2017 1
2019 1
2021 1
2022 1
2024 1

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25 results

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Page 1
A mouse model of Angelman syndrome imprinting defects.
Lewis MW, Vargas-Franco D, Morse DA, Resnick JL. Lewis MW, et al. Among authors: resnick jl. Hum Mol Genet. 2019 Jan 15;28(2):220-229. doi: 10.1093/hmg/ddy345. Hum Mol Genet. 2019. PMID: 30260400 Free PMC article.
The Diagnostic Journey of a Patient with Prader-Willi-Like Syndrome and a Unique Homozygous SNURF-SNRPN Variant; Bio-Molecular Analysis and Review of the Literature.
Pellikaan K, van Woerden GM, Kleinendorst L, Rosenberg AGW, Horsthemke B, Grosser C, van Zutven LJCM, van Rossum EFC, van der Lely AJ, Resnick JL, Brüggenwirth HT, van Haelst MM, de Graaff LCG. Pellikaan K, et al. Among authors: resnick jl. Genes (Basel). 2021 Jun 7;12(6):875. doi: 10.3390/genes12060875. Genes (Basel). 2021. PMID: 34200226 Free PMC article. Review.
Angelman syndrome imprinting center encodes a transcriptional promoter.
Lewis MW, Brant JO, Kramer JM, Moss JI, Yang TP, Hansen PJ, Williams RS, Resnick JL. Lewis MW, et al. Among authors: resnick jl. Proc Natl Acad Sci U S A. 2015 Jun 2;112(22):6871-5. doi: 10.1073/pnas.1411261111. Epub 2014 Nov 5. Proc Natl Acad Sci U S A. 2015. PMID: 25378697 Free PMC article.
Health Problems in Adults with Prader-Willi Syndrome of Different Genetic Subtypes: Cohort Study, Meta-Analysis and Review of the Literature.
Rosenberg AGW, Wellink CM, Tellez Garcia JM, Pellikaan K, Van Abswoude DH, Davidse K, Van Zutven LJCM, Brüggenwirth HT, Resnick JL, Van der Lely AJ, De Graaff LCG. Rosenberg AGW, et al. Among authors: resnick jl. J Clin Med. 2022 Jul 12;11(14):4033. doi: 10.3390/jcm11144033. J Clin Med. 2022. PMID: 35887798 Free PMC article.
25 results